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单个细胞中的二元基因诱导和蛋白质表达。

Binary gene induction and protein expression in individual cells.

作者信息

Zhang Qiang, Andersen Melvin E, Conolly Rory B

机构信息

Division of Computational Biology, CIIT Centers for Health Research, Research Triangle Park, NC 27709, USA.

出版信息

Theor Biol Med Model. 2006 Apr 5;3:18. doi: 10.1186/1742-4682-3-18.

Abstract

BACKGROUND

Eukaryotic gene transcription is believed to occur in either a binary or a graded fashion. With binary induction, a transcription activator (TA) regulates the probability with which a gene template is switched from the inactive to the active state without affecting the rate at which RNA molecules are produced from the template. With graded, also called rheostat-like, induction the gene template has continuously varying levels of transcriptional activity, and the TA regulates the rate of RNA production. Support for each of these two mechanisms arises primarily from experimental studies measuring reporter proteins in individual cells, rather than from direct measurement of induction events at the gene template.

METHODS AND RESULTS

In this paper, using a computational model of stochastic gene expression, we have studied the biological and experimental conditions under which a binary induction mode operating at the gene template can give rise to differentially expressed "phenotypes" (i.e., binary, hybrid or graded) at the protein level. We have also investigated whether the choice of reporter genes plays a significant role in determining the observed protein expression patterns in individual cells, given the diverse properties of commonly-used reporter genes. Our simulation confirmed early findings that the lifetimes of active/inactive promoters and half-lives of downstream mRNA/protein products are important determinants of various protein expression patterns, but showed that the induction time and the sensitivity with which the expressed genes are detected are also important experimental variables. Using parameter conditions representative of reporter genes including green fluorescence protein (GFP) and beta-galactosidase, we also demonstrated that graded gene expression is more likely to be observed with GFP, a longer-lived protein with low detection sensitivity.

CONCLUSION

The choice of reporter genes may determine whether protein expression is binary, graded or hybrid, even though gene induction itself operates in an all-or-none fashion.

摘要

背景

真核基因转录被认为以二元或分级方式发生。在二元诱导中,转录激活因子(TA)调节基因模板从无活性状态转换为活性状态的概率,而不影响从模板产生RNA分子的速率。在分级诱导(也称为变阻器样诱导)中,基因模板具有连续变化的转录活性水平,并且TA调节RNA产生的速率。对这两种机制的支持主要来自于在单个细胞中测量报告蛋白的实验研究,而不是来自于在基因模板上对诱导事件的直接测量。

方法与结果

在本文中,我们使用随机基因表达的计算模型,研究了在基因模板上运行的二元诱导模式在何种生物学和实验条件下能够在蛋白质水平上产生差异表达的“表型”(即二元、混合或分级)。鉴于常用报告基因的不同特性,我们还研究了报告基因的选择在确定单个细胞中观察到的蛋白质表达模式方面是否起重要作用。我们的模拟证实了早期的发现,即活性/非活性启动子的寿命和下游mRNA/蛋白质产物的半衰期是各种蛋白质表达模式的重要决定因素,但表明诱导时间和检测表达基因的灵敏度也是重要的实验变量。使用代表包括绿色荧光蛋白(GFP)和β-半乳糖苷酶在内的报告基因的参数条件,我们还证明,使用GFP(一种寿命较长、检测灵敏度较低的蛋白质)更有可能观察到分级基因表达。

结论

报告基因的选择可能决定蛋白质表达是二元、分级还是混合的,即使基因诱导本身以全或无的方式进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b21/1488830/1afacdbffa98/1742-4682-3-18-1.jpg

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